Archive
523 recalls were announced in August 2025.
Of the 523 recalls this month scored against our rubric, 7% are Critical, 20% are Severe.
Which agencies issued them
Kibbi is recalling 2024-2025 Renegade Verona and Verona LE recreational vehicles because a rear bracket may deflate the air suspension, increasing crash risk.
Fontaine Trailer Company is recalling 2025-2026 forklift trailers because misinstalled cables may disable the anti-lock brake system, increasing crash risk.
New Flyer is recalling specific electric bus models because an inadequate weld and software error may cause battery modules to overheat, increasing the risk of fire.
Motor Coach Industries is recalling specific 2020-2025 electric buses because an inadequate weld and software error may cause battery overheating and fire.
Altec is recalling certain 2011-2025 Aerial Device, Digger Derrick and Service Body vehicles because the cable step wire rope assembly may be improperly secured, allowing the entry step to detach.
Tuff Trailer USA is recalling 2024 TTA17200T and TTA18200T trailers because incorrect GVWR labels may lead to overloading and coupler failure.
Micro Bird is recalling 2025-2026 G5e school buses because the transmission interlock may allow the vehicle to move while the rear emergency door is locked, increasing injury risk.
Hiab USA Inc. is recalling specific Galfab reverse hoists because a mounting pin may fail, allowing the hoist to fall and increasing the risk of injury.
REV Recreation Group is recalling certain American Coach, American Eagle, American Dream and Fleetwood Palisade RVs because the waste tank macerator fuse may overheat and melt the fuse housing.
USDA FSIS issued a public health alert for Trader Joe's frozen pepperoni pizza imported from Italy without required reinspection. No illnesses have been reported.
About 764,000 Ryobi brushless electric pressure washers are recalled because the capacitor can overheat and burst, ejecting parts forcefully. There have been 41 reported explosions and 32 injuries.
Vermeer is recalling 2025 R600T trailers because the rear impact guards may have inadequate strength, increasing injury risk in crashes.
VinFast is recalling certain 2023-2025 VF8 vehicles because the Advanced Driver Assistance System may activate during wide turns, causing steering movements that are difficult for the driver to override.
Midwest Fire is recalling 2021-2025 All-Poly Series fire trucks because a mounting plate may crack, causing the hose reel to detach and creating a road hazard.
About 2.9 million electric motors used in gable- and roof-mounted attic fans are recalled because the safety cutoff may pose a short circuit and fire hazard. The firm has 159 reports of burning or fire; no injuries reported.
About 3,500 Lulive 12-drawer dressers are recalled because they are unstable if not anchored to the wall, posing tip-over and entrapment hazards, and they violate the STURDY Act standard. No incidents reported.
About 1,100 CT-ENERGY lithium coin battery chargers, model nc-02, are recalled because the coin batteries can be accessed easily by children and the packaging lacks child-resistance and the warnings required by Reese's Law.
Goodyear is recalling specific Metro Miler G652 tires because an inner liner defect may cause tire pressure loss, increasing crash risk.
About 6,000 DT Swiss carbon fiber road wheels are recalled because a defect can compromise the wheel's structural integrity, posing a crash hazard. Six reports of carbon layer separation; no injuries reported.
About 10,100 Party Favors lite-up torches and mini laser pointers are recalled because their button cell batteries can be accessed easily by children, in violation of mandatory standards. No incidents reported.
About 12,600 Nimbus Lock Carabiners are recalled because the automatic closing mechanism can break and prevent the gate from closing, posing a fall risk. There are 21 reports of breakage; no injuries reported.
Hillside Orchard Farms Banana Nut Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Cinnamon Pecan Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Jalapeno Cheese Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Cheese Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
RELIANCE 4-FRONT defibrillation leads are recalled because affected models may show gradually rising LVSI measurements linked to calcification of the defibrillation coils, which may lead to early lead replacement.
Hillside Orchard Farms Fresh Apple Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
ENDOTAK RELIANCE G/SG defibrillation leads with the 4-SITE connector are recalled because affected models may show gradually rising LVSI measurements linked to calcification of the defibrillation coils.
Hillside Orchard Farms Blueberry Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Strawberry Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Fresh Peach Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Peach Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Strawberry Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Apple Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hillside Orchard Farms Cinnamon Pecan Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
Hamilton C6 ventilators are recalled over a mechanical defect on a printed circuit board that may cause the device to fail at startup or interrupt ventilation during use. 1,040 systems are affected.
Hillside Orchard Farms Blueberry Fritters, 7 oz, are recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
ENDOTAK RELIANCE G/SG transvenous defibrillation leads are recalled because affected models may show gradually rising LVSI measurements linked to calcification of the defibrillation coils.
Hillside Orchard Farms Fresh Blackberry Bread, 23 oz, is recalled for undeclared egg. The FDA classified the action as Class I, its most serious category.
BMW is recalling certain 2026 X5, X5 Plug-in Hybrid, and X7 vehicles because the windshield may not be sealed properly, allowing water to enter electrical components and potentially causing headlight failure or fire.
Carvedilol Tablets USP, 12.5 mg, packaged by Major Pharmaceuticals, lot T05693, are recalled nationwide because N-Nitroso Carvedilol Impurity-1 exceeded the FDA-recommended 4.0 ppm limit. 26,628 cartons are affected.
The ESG-410 Electrosurgical Generator is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 155 units are affected.
Imported Frozen Half Shell Oysters in 15-pound boxes, lot B250123, are recalled because they are potentially contaminated with norovirus. 828 cartons are affected.
Hospira Epinephrine Injection USP, 1 mg/10 mL, lots LY3681, LY4360 and LY4416, is recalled nationwide for lack of assurance of sterility. 49,620 vials are affected.
Imported Frozen Half Shell Oysters in 15-pound boxes, lot B250112, are recalled because they are potentially contaminated with norovirus. 98 cartons are affected.
Hospira 8.4% Sodium Bicarbonate Injection USP, 50 mEq/50 mL, lot LH2671, is recalled nationwide for lack of assurance of sterility. 15,750 vials are affected.
Raw Ramen Noodle HA #22W (4942) in 10 lb bulk cases, made by Kobayashi Noodle USA, is recalled because the label does not declare soy as the source of the lecithin ingredient. 2,800 cases are affected.
Raw Ramen Noodle HA #22W in 10 lb bulk cases, made by Kobayashi Noodle USA, is recalled because the label does not declare soy as the source of the lecithin ingredient. 945 cases are affected.
Sri Sri Tattva Ojasvita Chocomalt, 7 oz / 200 g paper pouches, is recalled because it contains undeclared soy lecithin. 1,100 units are affected.
7up Zero Sugar Tropical Soda in 12 fl oz cans is recalled because the cans are labeled Zero Sugar but contain full sugar product. 1,954 cases are affected.
Burr Hole Cover Kits used with the Vercise Deep Brain Stimulation System are recalled because resistance closing the retaining clip may cause procedural delay or lead migration requiring further surgery. 24,583 units are affected.
The ESG-410 Legacy Electrosurgical Generator, model WA91307C, is recalled because it may display an E0662 System Error followed by a single automatic reboot or a continuous reboot loop. 434 units are affected.
Estrone RIA kits, catalog number DSL8700, are recalled because certain lots may rarely give falsely high or falsely low patient results. 279 units are affected.
Biscuit Mix packed exclusively for Chick-fil-A, Inc. in 2.625 lb bags is recalled for undeclared eggs. The recall covers 150 cases of 12 bags.
BZK Antiseptic Towelettes containing benzalkonium chloride 0.13%, sold 100 per carton for professional use, are recalled for lack of assurance of sterility. The recall covers 3.85 million cartons.
Pentax Medical EPK-i8020c video processors are recalled after reports of darkened images, smoke-like steam and a hot endoscope light guide that may cause thermal injury to the patient's mucous membrane. 144 units are affected.
OtoLase Starter Kits, UPN AC-2003748, batches 32644549 and 32769567, are recalled because finished product labeled as sterile may not have been sterilized. 13 units are affected.
Bayonet Luer-Lock injection needles, models 50-353-23 and 50-345-23, are recalled because affected product showed elevated cytotoxicity values, which may present a risk of intolerance or allergic reaction.
Tavaborole Topical Solution 5%, 10 mL bottles from lot T401968, distributed by Viona Pharmaceuticals, is recalled because of discoloration. 3,960 bottles are affected.
Cipla Albuterol Sulfate Inhalation Aerosol, 90 mcg, lot 4IB0519, is recalled nationwide after out-of-specification particle size distribution results at the 12-month stability point. 20,352 packs are affected.
Dynex Agility Sample Tips, model 67910 lot 863366, are recalled because the internal rack label reads reagent tip rack, causing the instrument to misidentify the tips and preventing their use. 237 units are affected.
DRS Vascular is recalling 264 Q-Stop Suture Retention Devices. The FDA enforcement record for this action carries a placeholder in place of a stated reason for the recall.
Clearview Strep A Exact II Dipstick Respiratory Kits are recalled because a classification error in the inventory system sent devices to customers without the required license to buy them. 5 kits are affected.
VITROS Chemistry Products Ca Slides, catalog number 145 0261, generations 67 and above, are recalled because calibration failures on VITROS XT systems delay calcium test results. 174,215 units are affected.
Sensodyne Pronamel Active Shield toothpaste is recalled for a label mix-up: the outer carton reads Fresh Mint while the tube reads Cool Mint/Whitening. The toothpaste inside is Fresh Mint, as the carton states.
Forest River is recalling certain 2018-2026 Riverstone fifth wheel trailers because the steel hydraulic brake lines may fail and leak brake fluid, causing a loss of brake function.
Polestar is recalling certain 2025 Polestar 3 vehicles because the hood wing front bumper may be missing bolts, allowing the bumper to detach and become a road hazard.
Chrysler is recalling specific Mopar rearview camera modules because cracks in the microprocessor may prevent the image from displaying properly, increasing crash risk.
Chrysler is recalling certain 2019-2021 Ram ProMaster and 2019-2020 Dodge Journey vehicles because cracks in the microprocessor may stop the rearview camera image displaying properly.
Tiffin Motorhomes is recalling 2025 GT1 Touring vans because rear seat belt buckles may be too short to fasten, increasing injury risk in a crash.
Forest River is recalling 2026 Cedar Creek recreational trailers because they may lack an emergency exit window, posing a risk of injury during an emergency.
Nova Bus is recalling 2013 LFS transit buses because coolant hoses may leak hot liquid into the passenger area, posing a burn risk.
Hyundai is recalling certain 2025–2026 Tucson and Santa Fe vehicles because engine connecting rod bolts may have been improperly tightened, risking loss of drive power, engine damage, oil leaks, and potential fire.
Kia is recalling certain 2025 K4 and Sorento vehicles because the connecting rod bolts in the engine may have been improperly tightened, which can cause a loss of drive power.
Keystone RV Company is recalling 2026 Springdale and Hideout travel trailers because pivot brackets on the bunk bed may bend or break, posing a risk of injury.
Truck Certification Services is recalling specific Load Carrying Capacity labels where weight units may be reversed, potentially leading to vehicle overloading.
ZF North America is recalling specific steering columns because improperly tightened bolts may cause steering components to separate, increasing the risk of a crash.
Ford is recalling specific Edge and Lincoln MKX vehicles because the rear brake jounce hose may rupture, causing a brake fluid leak that increases stopping distance.
Forest River is recalling certain 2024-2026 East to West Entrada recreational vehicles because an incorrectly wired 7-way harness may cause the trailer brakes to lock up when the RV brakes are applied.
New Flyer is recalling certain 2012-2025 Xcelsior buses that may have been built without enough emergency exits, or with exits in an incorrect location. This fails FMVSS 217.
Ford is recalling 2024-2026 Ranger vehicles because side curtain air bags may tear during deployment, increasing injury risk.
Forest River is recalling certain 2026 Flagstaff and Rockwood recreational trailers because the breakaway switch was wired to the incorrect side of the battery disconnect switch, making it inoperative. An inoperative breakaway switch increases the risk of a crash.
Ford is recalling certain 2024-2025 Mustang and Mustang GTD vehicles because water may enter the body control module and cut communication with the licence plate, side marker and tail lights.
Ford is recalling certain 2025–2026 F-150, F-250 SD, F-350 SD, F-450 SD, and F-550 SD vehicles because the instrument panel cluster may fail at startup, preventing display of critical information like warning lights and vehicle speed.
Ford is recalling certain 2025 Explorer and Lincoln Aviator vehicles because an improperly manufactured body control module may leave a towed trailer's tail lights unlit. This fails FMVSS 108.
Rivian is recalling certain 2025 R1S and R1T vehicles because an improperly grounded connection inside the High Voltage Distribution Box may cause a loss of drive power.
International is recalling certain 2026 MV vehicles because the battery interconnect cable may contact the auxiliary stud and hold down bracket, causing a short circuit.
About 1,100 IBC CX-199 and CX-150 combi boilers are recalled because the hot water can exceed the temperature set on the control panel, posing a burn hazard. No injuries have been reported.
General Motors is recalling certain 2023-2026 Corvette vehicles with a left-side radiator/fan combination because excess fuel may spill into the filler pocket during refuelling and leak onto an ignition source.
Aluminum Trailer Company is recalling certain 2023-2025 trailers because a software error may cause the radio and speakers to overheat, increasing the risk of fire.
Randalls Salad Sandwich 16 Inch Trays are recalled for potential Listeria monocytogenes contamination. The FDA classified the action as Class I, its most serious category.
Jewel Osco Club Sandwiches with Salad are recalled for potential Listeria monocytogenes contamination. The FDA classified the action as Class I, its most serious category.
Ready Meals Tuna Salad Over Bed of Lettuce is recalled for potential Listeria monocytogenes contamination. The FDA classified the action as Class I, its most serious category.
Randalls Premium Tuna Salad is recalled for potential Listeria monocytogenes contamination. The FDA classified the action as Class I, its most serious category.
Ready Meals Tuna Salad is recalled for potential Listeria monocytogenes contamination. The FDA classified the action as Class I, its most serious category.
Baxter is issuing an urgent correction for 36,705 Novum IQ large volume pumps because the pump may underinfuse when moving to a flow rate more than double the current one.
Certain batches of the Carotid WALLSTENT Monorail Endoprosthesis are being removed after complaints of greater than anticipated resistance withdrawing the delivery system. The most serious potential consequence is stroke.
Randalls Salad Sandwich 12 Inch Trays are recalled for potential Listeria monocytogenes contamination. The FDA classified the action as Class I, its most serious category.
Reser's Tuna Salad in 5 lb foodservice tubs, the version containing pickle relish, is recalled for potential Listeria monocytogenes contamination from recalled breadcrumbs. 108 cases are affected.
Quesito El Establo brand Quesito Colombiano, 1 lb, is recalled because it was made and held under insanitary conditions and may be contaminated with Listeria monocytogenes. All product codes are affected.
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